Oxime Analogs of Amino Acids and Peptides Are Efficient Ligands for Ni(II) Ions

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dc.contributor.authorOnindo, Charles O.
dc.contributor.authorSliva, Tatiana Yu.
dc.contributor.authorKowalik-Jankowska, Teresa
dc.contributor.authorAmirkhanov, Vladimir M.
dc.contributor.authorGo̵wiak, Tadeusz
dc.contributor.authorFritskii, Igor O.
dc.contributor.authorKozo̵wski, Henryk
dc.date.accessioned2013-10-07T11:44:32Z
dc.date.available2013-10-07T11:44:32Z
dc.date.issued1997-03
dc.description.abstractOxime derivatives of amino acids, amides, and peptides are very efficient ligands for NiII ions forming very stable water-soluble complexes. Oxime of amino acids amides forms octahedral and square-planar complexes with the same 4N coordination mode. The spectroscopic and X-ray diffraction studies indicate an unusual role for the hydrogen bond in NiH−1L2 species, which stabilizes the cis coordination of two ligands in a planar complex. Oxime analogs of natural amino acid can be much more efficient ligands than the parent molecules.en_US
dc.identifier.citationJournal of Inorganic Biochemistry Volume 65, Issue 4, March 1997, Pages 287–294en_US
dc.identifier.urihttp://ir-library.ku.ac.ke/handle/123456789/7422
dc.language.isoenen_US
dc.publisherJournal of Inorganic Biochemistryen_US
dc.titleOxime Analogs of Amino Acids and Peptides Are Efficient Ligands for Ni(II) Ionsen_US
dc.typeArticleen_US
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